Canonical Allele Identifier: CA412150541
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489823T>A , CM000684.2:g.50489823T>A GRCh38
NC_000022.10:g.50928252T>A , CM000684.1:g.50928252T>A GRCh37
NC_000022.9:g.49275118T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.825T>A MANE Select ENSP00000216075.6:p.Ile275=
ENST00000216075.10:c.825T>A ENSP00000216075.6:p.Ile275=
ENST00000395732.7:c.811T>A ENSP00000379081.3:p.Ter271Arg
ENST00000395733.7:c.694T>A ENSP00000379082.3:p.Ter232Arg
ENST00000451761.1:c.765T>A ENSP00000409894.1:p.Ile255=
NM_017584.5:c.825T>A NP_060054.4:p.Ile275=
XM_005261925.3:c.687T>A XP_005261982.1:p.Ile229=
XR_244455.2:n.3321T>A
XM_005261925.4:c.687T>A XP_005261982.1:p.Ile229=
NM_017584.6:c.825T>A MANE Select NP_060054.4:p.Ile275=